rs121913407

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(T;T)	0	common in clinvar

Make rs121913407(C;C)

Make rs121913407(C;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

41224645

Gene

CTNNB1

is a	snp
is	mentioned by
dbSNP	rs121913407
dbSNP (classic)	rs121913407
ClinGen	rs121913407
ebi	rs121913407
HLI	rs121913407
Exac	rs121913407
Gnomad	rs121913407
Varsome	rs121913407
LitVar	rs121913407
Map	rs121913407
PheGenI	rs121913407
Biobank	rs121913407
1000 genomes	rs121913407
hgdp	rs121913407
ensembl	rs121913407
geneview	rs121913407
scholar	rs121913407
google	rs121913407
pharmgkb	rs121913407
gwascentral	rs121913407
openSNP	rs121913407
23andMe	rs121913407
SNPshot	rs121913407
SNPdbe	rs121913407
MSV3d	rs121913407
GWAS Ctlg	rs121913407

Max Magnitude

0

OMIM	116806
Desc
Variant	0014
Related	also

ClinVar
Risk	rs121913407(C;C) rs121913407(G;G)
Alt	rs121913407(C;C) rs121913407(G;G)
Reference	Rs121913407(T;T)
Significance	Other
Disease	Hepatocellular carcinoma not provided Adrenocortical carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Adenocarcinoma of prostate Malignant melanoma of skin Malignant melanoma Colorectal Neoplasms Disease Transitional cell carcinoma of the bladder Neoplasm of brain
Variation	info
Gene	CTNNB1
CLNDBN	Hepatocellular carcinoma not provided Adrenocortical carcinoma Malignant neoplasm of body of uterus Adenocarcinoma of lung Adenocarcinoma of prostate Malignant melanoma of skin Malignant melanoma Colorectal Neoplasms Disease Transitional cell carcinoma of the bladder Neoplasm of brain
Reversed	0
HGVS	NC_000003.11:g.41266136T>C; NC_000003.11:g.41266136T>G
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000019154.5, RCV000087197.2, RCV000417674.1, RCV000422223.1, RCV000423471.1, RCV000427866.1, RCV000428983.1, RCV000435313.1, RCV000439398.1, RCV000439866.1, RCV000441996.1, RCV000420592.1, RCV000427795.1,